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Will Climate Change, Genetic and Demographic Variation Or Rat Predation Pose the Greatest Risk for Persistence of an Altitudinally Distributed Island Endemic?
Biology 2012, 1, 736-765; doi:10.3390/biology1030736 OPEN ACCESS biology ISSN 2079-7737 www.mdpi.com/journal/biology Article Will Climate Change, Genetic and Demographic Variation or Rat Predation Pose the Greatest Risk for Persistence of an Altitudinally Distributed Island Endemic? Catherine Laura Simmons 1, Tony D. Auld 2, Ian Hutton 3, William J. Baker 4 and Alison Shapcott 1,* 1 Faculty of Science Health, Education and Engineering, University of the Sunshine Coast, Maroochydore DC, QLD 4558, Australia; E-Mail: [email protected] 2 Office of Environment and Heritage (NSW), P.O. Box 1967 Hurstville, NSW 2220, Australia; E-Mail: [email protected] 3 P.O. Box 157, Lord Howe Island, NSW 2898, Australia; E-Mail: [email protected] 4 Royal Botanic Gardens, Kew, Richmond, Surrey, TW9 3AB, UK; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +61-7-5430-1211; Fax: +61-7-5430-2881. Received: 3 September 2012; in revised form: 29 October 2012 / Accepted: 16 November 2012 / Published: 23 November 2012 Abstract: Species endemic to mountains on oceanic islands are subject to a number of existing threats (in particular, invasive species) along with the impacts of a rapidly changing climate. The Lord Howe Island endemic palm Hedyscepe canterburyana is restricted to two mountains above 300 m altitude. Predation by the introduced Black Rat (Rattus rattus) is known to significantly reduce seedling recruitment. We examined the variation in Hedyscepe in terms of genetic variation, morphology, reproductive output and demographic structure, across an altitudinal gradient. -
Studies on Phytoconstituents, in Vitro Antioxidant and Cytotoxity Activity of Harpullia Arborea Bark Extracts on Human Epidermoid Larynx Carcinoma Cell Line (Hep-2) R
The International journal of analytical and experimental modal analysis ISSN NO: 0886-9367 Studies on Phytoconstituents, In vitro Antioxidant and Cytotoxity Activity of Harpullia arborea Bark Extracts on Human Epidermoid Larynx Carcinoma Cell Line (HEp-2) R. Rajeswari1, S. Murugesh1*, D. Jegadeeshkumar2, B. Prakash3, V. Vinoth kumar4 1Department of Botany, School of Life Sciences, Periyar University, Periyar Palkalai Nagar, Salem-636 011, Tamil Nadu, India. 2Chromopark Research Centre, Namakkal - 637001 Tamil Nadu, India. 3Department of Biotechnology, School of Life Sciences, Vels Institute of Science Technology & Advanced Studies, Chennai, Tamil Nadu, India. 4Department of Microbiology, Sree Narayana Guru College, Coimbatore-641105, India. *Corresponding Author Email: [email protected] Phone: +91 9943364913 ORCID: 0000-0002-8382-8553 Abstract Cancer is major public issues and one of the leading causes of death in prosperous countries. Traditional plants are a valued source of novel cytotoxic agents and are still in performance better role in health concern. In the present study, the bark of methanol and chloroform extracts were subjected to preliminary phytochemicals screening was done using different biochemical tests. Among the 2 solvent extracts, methanol showed the highest number of phytochemicals, which extract was subjected to in vitro study of antioxidant activity by DPPH method and cytotoxicity activity against HEp-2 cell lines by MTT assay. Furthermore, DNA fragmentation and GCMS analysis were subjected. By the analsyis, following phyto-constituents like tannins, saponins, Steroids, Carbohydrate and Phenols, Flavonoids, Terpenoids, and quinine were observed. The methanol extract was found to be selectively cytotoxic in vitro to HEp-2 cell lines with IC50values was15.6 µg/ml. -
Brisbane Native Plants by Suburb
INDEX - BRISBANE SUBURBS SPECIES LIST Acacia Ridge. ...........15 Chelmer ...................14 Hamilton. .................10 Mayne. .................25 Pullenvale............... 22 Toowong ....................46 Albion .......................25 Chermside West .11 Hawthorne................. 7 McDowall. ..............6 Torwood .....................47 Alderley ....................45 Clayfield ..................14 Heathwood.... 34. Meeandah.............. 2 Queensport ............32 Trinder Park ...............32 Algester.................... 15 Coopers Plains........32 Hemmant. .................32 Merthyr .................7 Annerley ...................32 Coorparoo ................3 Hendra. .................10 Middle Park .........19 Rainworth. ..............47 Underwood. ................41 Anstead ....................17 Corinda. ..................14 Herston ....................5 Milton ...................46 Ransome. ................32 Upper Brookfield .......23 Archerfield ...............32 Highgate Hill. ........43 Mitchelton ...........45 Red Hill.................... 43 Upper Mt gravatt. .......15 Ascot. .......................36 Darra .......................33 Hill End ..................45 Moggill. .................20 Richlands ................34 Ashgrove. ................26 Deagon ....................2 Holland Park........... 3 Moorooka. ............32 River Hills................ 19 Virginia ........................31 Aspley ......................31 Doboy ......................2 Morningside. .........3 Robertson ................42 Auchenflower -
Origins and Assembly of Malesian Rainforests
ES50CH06_Kooyman ARjats.cls October 21, 2019 11:31 Annual Review of Ecology, Evolution, and Systematics Origins and Assembly of Malesian Rainforests Robert M. Kooyman,1,2 Robert J. Morley,3,4 Darren M. Crayn,5 Elizabeth M. Joyce,5 Maurizio Rossetto,2 J.W. Ferry Slik,6 Joeri S. Strijk,7,8,9 Ta o S u , 9,10 Jia-Yee S. Yap,2,11 and Peter Wilf12 1Department of Biological Sciences, Macquarie University, Sydney, New South Wales 2109, Australia; email: [email protected] 2National Herbarium of New South Wales, Royal Botanic Gardens and Domain Trust, Sydney, New South Wales 2000, Australia 3Palynova UK, Littleport, Cambridgeshire CB6 1PY, United Kingdom 4Earth Sciences Department, Royal Holloway, University of London, Egham, Surrey TW20 0EX, United Kingdom 5Australian Tropical Herbarium and Centre for Tropical Environmental Sustainability Science, James Cook University, Smithfield, Queensland 4878, Australia 6Environmental and Life Sciences, Faculty of Science, Universiti Brunei Darussalam, Gadong BE1410, Brunei Darussalam 7State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, College of Forestry, Guangxi University, Nanning, Guangxi 530005, China 8Alliance for Conservation Tree Genomics, Pha Tad Ke Botanical Garden, 06000 Luang Prabang, Lao PDR 9Key Laboratory of Tropical Forest Ecology, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Mengla 666303, China 10Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences, Yezin, Nay Pyi Taw 05282, Myanmar Access provided by 118.208.177.216 on 11/06/19. For personal use only. 11Queensland Alliance of Agriculture and Food Innovation, University of Queensland, Brisbane, Queensland 4072, Australia 12Department of Geosciences, Pennsylvania State University, University Park, Annu. -
How Sympatric Is Speciation in the Howea Palms of Lord Howe Island?
Molecular Ecology (2009) 18, 3629–3638 doi: 10.1111/j.1365-294X.2009.04306.x How sympatric is speciation in the Howea palms of Lord Howe Island? WIESŁAW BABIK,*†† ROGER K. BUTLIN,† WILLIAM J. BAKER,‡ ALEXANDER S. T. PAPADOPULOS,* MATTHIEU BOULESTEIX,* MARIE-CHARLOTTE ANSTETT,§ CHRISTIAN LEXER,*– IAN HUTTON** and VINCENT SAVOLAINEN*‡ *Imperial College London, Silwood Park, Ascot, Berkshire SL5 7PY, UK, †Department of Animal and Plant Sciences, University of Sheffield, Sheffield S10 2TN, UK, ‡Royal Botanic Gardens, Kew, Richmond, Surrey TW9 3DS, UK, §Centre for Evolutionary and Functional Ecology, UMR 5175, 34293 Montpellier cedex 5, France, –University of Fribourg, Department of Biology, CH-1700 Fribourg, Switzerland, **Lord Howe Island, PO Box 157, New South Wales 2898, Australia Abstract The two species of the palm genus Howea (Arecaceae) from Lord Howe Island, a minute volcanic island in the Tasman Sea, are now regarded as one of the most compelling examples of sympatric speciation, although this view is still disputed by some authors. Population genetic and ecological data are necessary to provide a more coherent and comprehensive understanding of this emerging model system. Here, we analyse data on abundance, juvenile recruitment, pollination mode and genetic variation and structure in both species. We find that Howea forsteriana is less abundant than Howea belmoreana. The genetic data based on amplified fragment length polymorphisms markers indicate similar levels of variation in the two species, despite the estimated census population size of H. belmoreana being three times larger than that of H. forsteriana. Genetic structure within species is low although some weak isolation by distance is detectable. -
Cunninghamia Date of Publication: April 2020 a Journal of Plant Ecology for Eastern Australia
Cunninghamia Date of Publication: April 2020 A journal of plant ecology for eastern Australia ISSN 0727- 9620 (print) • ISSN 2200 - 405X (Online) A Systematic Flora Survey, Floristic Classification and High-Resolution Vegetation Map of Lord Howe Island Paul Sheringham 1*, Peter Richards2, Phil Gilmour3, Jill Smith1 and Ernst Kemmerer 4 1 Department of Planning, Industry and Environment, Locked Bag 914 COFFS HARBOUR NSW 2450 2 17 Coronation Avenue, SAWTELL NSW 2452 3 523 Roses Rd, GLENIFFER, NSW 2454 4 Cradle Coast NRM, PO Box 338, BURNIE TAS 7320 * Author for correspondence: [email protected] Abstract: The present study took advantage of the availability of high resolution ADS40 digital imagery to 1) systematically resample the vegetation of the Lord Howe Island Group (LHIG, excluding Ball’s Pyramid); 2) conduct a numerical analysis of the floristic data; 3) map vegetation extent and the distribution of vegetation communities and 4) compare the resultant classification and mapping with those of Pickard (1983). In July 2013, a total of 86 full floristic and 105 rapid floristic sites were sampled across the island, based on a stratified random sampling design. A hierarchical agglomerative clustering strategy (Flexible UPGMA) and Bray-Curtis dissimilarity coefficient with default beta, along with nearest neighbour analysis to identify anomalous site allocations, was used to analyze the floristic data. In total 33 vegetation communities were delineated and mapped: 19 mapping units from the full floristic analysis; 7 variants identified within five of the above 19 groups; 3 mapping units from analysis of canopy- only floristic data; and 4 mapping units recognised in previous studies that are mapped but were not sampled in this survey. -
Green & Healthy Hawaii: Identifying & Introducing Alternative Ornamental
Final Report Green & Healthy Hawaii: Identifying & Introducing Alternative Ornamental Landscape Plants in Response to Invasive Species Issues By Dr. Andy Kaufman (PI) Dr. Richard Criley (CO-PI) Dr Linda Cox (CO-PI) Alberto H. Ricordi, M.Sc. (Graduate Assistant) Tropical Landscape and Human Interaction Lab Department of Tropical Plant and Soil Sciences University of Hawaii at Manoa Funded by a grant from: Hawaii Invasive Species Council (HISC) Green & Healthy Hawaii: Identifying & Introducing Alternative Ornamental Landscape Plants in Response to Invasive Species Issues Abstract ........................................................................................................................... 4 Introduction ..................................................................................................................... 4 Problem statement .......................................................................................................... 6 Objectives ....................................................................................................................... 6 Goals ............................................................................................................................... 7 Materials and Methods .................................................................................................... 7 Selection of Invasive Species ...................................................................................... 9 Selection of Alternative Species ............................................................................... -
Accepted Manuscript
Accepted Manuscript Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal levels in the soapberry family (Sapindaceae) Sven Buerki, Félix Forest, Pedro Acevedo-Rodríguez, Martin W. Callmander, Johan A.A. Nylander, Mark Harrington, Isabel Sanmartín, Philippe Küpfer, Nadir Alvarez PII: S1055-7903(09)00017-7 DOI: 10.1016/j.ympev.2009.01.012 Reference: YMPEV 3130 To appear in: Molecular Phylogenetics and Evolution Received Date: 21 May 2008 Revised Date: 27 November 2008 Accepted Date: 23 January 2009 Please cite this article as: Buerki, S., Forest, F., Acevedo-Rodríguez, P., Callmander, M.W., Nylander, J.A.A., Harrington, M., Sanmartín, I., Küpfer, P., Alvarez, N., Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal levels in the soapberry family (Sapindaceae), Molecular Phylogenetics and Evolution (2009), doi: 10.1016/j.ympev.2009.01.012 This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. ACCEPTED MANUSCRIPT Buerki et al. 1 1 Plastid and nuclear DNA markers reveal intricate relationships at subfamilial and tribal 2 levels in the soapberry family (Sapindaceae) 3 4 Sven Buerki a,*, Félix Forest b, Pedro Acevedo-Rodríguez c, Martin W. Callmander d,e, 5 Johan A. -
I Is the Sunda-Sahul Floristic Exchange Ongoing?
Is the Sunda-Sahul floristic exchange ongoing? A study of distributions, functional traits, climate and landscape genomics to investigate the invasion in Australian rainforests By Jia-Yee Samantha Yap Bachelor of Biotechnology Hons. A thesis submitted for the degree of Doctor of Philosophy at The University of Queensland in 2018 Queensland Alliance for Agriculture and Food Innovation i Abstract Australian rainforests are of mixed biogeographical histories, resulting from the collision between Sahul (Australia) and Sunda shelves that led to extensive immigration of rainforest lineages with Sunda ancestry to Australia. Although comprehensive fossil records and molecular phylogenies distinguish between the Sunda and Sahul floristic elements, species distributions, functional traits or landscape dynamics have not been used to distinguish between the two elements in the Australian rainforest flora. The overall aim of this study was to investigate both Sunda and Sahul components in the Australian rainforest flora by (1) exploring their continental-wide distributional patterns and observing how functional characteristics and environmental preferences determine these patterns, (2) investigating continental-wide genomic diversities and distances of multiple species and measuring local species accumulation rates across multiple sites to observe whether past biotic exchange left detectable and consistent patterns in the rainforest flora, (3) coupling genomic data and species distribution models of lineages of known Sunda and Sahul ancestry to examine landscape-level dynamics and habitat preferences to relate to the impact of historical processes. First, the continental distributions of rainforest woody representatives that could be ascribed to Sahul (795 species) and Sunda origins (604 species) and their dispersal and persistence characteristics and key functional characteristics (leaf size, fruit size, wood density and maximum height at maturity) of were compared. -
WRA Species Report
Family: Arecaceae Taxon: Howea forsteriana Synonym: Common Name Kentia palm Sentry palm Questionaire : current 20090513 Assessor: Chuck Chimera Designation: EVALUATE Status: Assessor Approved Data Entry Person: Chuck Chimera WRA Score 3 101 Is the species highly domesticated? y=-3, n=0 n 102 Has the species become naturalized where grown? y=1, n=-1 103 Does the species have weedy races? y=1, n=-1 201 Species suited to tropical or subtropical climate(s) - If island is primarily wet habitat, then (0-low; 1-intermediate; 2- High substitute "wet tropical" for "tropical or subtropical" high) (See Appendix 2) 202 Quality of climate match data (0-low; 1-intermediate; 2- High high) (See Appendix 2) 203 Broad climate suitability (environmental versatility) y=1, n=0 n 204 Native or naturalized in regions with tropical or subtropical climates y=1, n=0 y 205 Does the species have a history of repeated introductions outside its natural range? y=-2, ?=-1, n=0 y 301 Naturalized beyond native range y = 1*multiplier (see y Appendix 2), n= question 205 302 Garden/amenity/disturbance weed n=0, y = 1*multiplier (see Appendix 2) 303 Agricultural/forestry/horticultural weed n=0, y = 2*multiplier (see n Appendix 2) 304 Environmental weed n=0, y = 2*multiplier (see n Appendix 2) 305 Congeneric weed n=0, y = 1*multiplier (see Appendix 2) 401 Produces spines, thorns or burrs y=1, n=0 n 402 Allelopathic y=1, n=0 n 403 Parasitic y=1, n=0 n 404 Unpalatable to grazing animals y=1, n=-1 405 Toxic to animals y=1, n=0 n 406 Host for recognized pests and pathogens y=1, -
(Arecaceae): Évolution Du Système Sexuel Et Du Nombre D'étamines
Etude de l’appareil reproducteur des palmiers (Arecaceae) : évolution du système sexuel et du nombre d’étamines Elodie Alapetite To cite this version: Elodie Alapetite. Etude de l’appareil reproducteur des palmiers (Arecaceae) : évolution du système sexuel et du nombre d’étamines. Sciences agricoles. Université Paris Sud - Paris XI, 2013. Français. NNT : 2013PA112063. tel-01017166 HAL Id: tel-01017166 https://tel.archives-ouvertes.fr/tel-01017166 Submitted on 2 Jul 2014 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. UNIVERSITE PARIS-SUD ÉCOLE DOCTORALE : Sciences du Végétal (ED 45) Laboratoire d'Ecologie, Systématique et E,olution (ESE) DISCIPLINE : -iologie THÈSE DE DOCTORAT SUR TRAVAUX soutenue le ./05/10 2 par Elodie ALAPETITE ETUDE DE L'APPAREIL REPRODUCTEUR DES PAL4IERS (ARECACEAE) : EVOLUTION DU S5STE4E SE6UEL ET DU NO4-RE D'ETA4INES Directeur de thèse : Sophie NADOT Professeur (Uni,ersité Paris-Sud Orsay) Com osition du jury : Rapporteurs : 9ean-5,es DU-UISSON Professeur (Uni,ersité Pierre et 4arie Curie : Paris VI) Porter P. LOWR5 Professeur (4issouri -otanical Garden USA et 4uséum National d'Histoire Naturelle Paris) Examinateurs : Anders S. -ARFOD Professeur (Aarhus Uni,ersity Danemark) Isabelle DA9OA Professeur (Uni,ersité Paris Diderot : Paris VII) 4ichel DRON Professeur (Uni,ersité Paris-Sud Orsay) 3 4 Résumé Les palmiers constituent une famille emblématique de monocotylédones, comprenant 183 genres et environ 2500 espèces distribuées sur tous les continents dans les zones tropicales et subtropicales. -
Conservation Issues for the Vascular Flora of Lord Howe Island
490 Cunninghamia 8(4): 2004 Auld & Hutton, Plant conservation on Lord Howe Island Conservation issues for the vascular flora of Lord Howe Island Tony D. Auld1 and Ian Hutton2 1Biodiversity and Conservation Science Section, Department of Environment and Conservation (NSW) PO Box 1967 Hurstville NSW 2220, AUSTRALIA Email: [email protected] 2PO Box 157 Lord Howe Island, NSW 2898 AUSTRALIA Abstract: The flora of the Lord Howe Island Group (31°30’S, 159°05’E) comprises a unique mix of elements of Australian, New Zealand and New Caledonian floras. It is significant for its high degree of endemism and for its structural and biological (leaves, flowers, fruit) role in supporting a diverse array of fauna. Conservation of this flora is dependant upon: reducing current habitat degradation (mostly the result of exotic weeds); minimising any future impacts, in particular the effects of climate change on the unique cloud forests of the southern mountains and the continued introduction and spread of weeds and the pathogen Phytophthora cinnamomi. We provide a description of the nature of the major threats to the flora and suggest an area-based scheme, focussed on the relative conservation significance of remaining vegetation, as a mechanism for developing priorities for threat mitigation activities. While a number of threat control works are in place, eg. weed control, some re-emphasis is needed. In addition, some new initiatives are required including: reducing the rate of introductions of new exotics; a system to remove potential environmental weeds from the settlement area; phytosanitary guidelines; pathogen quarantine measures; search and removal of environmental weeds from remote areas; and ex situ initiatives for plant species restricted to the cloud forests of the southern mountains.